Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@@H](OC2=C([C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C3=C(C=C2)C(=O)C(=CO3)C2=CC=C(O)C=C2)[C@H](O)[C@@H](O)[C@@H]1O

InChIKey

InChIKey=XDEZHFNQHUKPOB-WIQAIWCDSA-N

Formula

C27H30O14

Mass

578.523

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Isoflavonoids

Subclass

Isoflavonoid O-glycosides

Intermediate Tree Nodes

Not available

Direct Parent

Isoflavonoid O-glycosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Isoflavonoid-7-o-glycoside - Isoflavonoid o-glycoside - Isoflavonoid-8-c-glycoside - Isoflavonoid c-glycoside - Isoflavone - Phenolic glycoside - O-glycosyl compound - C-glycosyl compound - Glycosyl compound - Chromone - Benzopyran - 1-benzopyran - Pyranone - Phenol - 1-hydroxy-2-unsubstituted benzenoid - Monosaccharide - Pyran - Monocyclic benzene moiety - Benzenoid - Oxane - Heteroaromatic compound - Secondary alcohol - Acetal - Oxacycle - Dialkyl ether - Ether - Organoheterocyclic compound - Polyol - Alcohol - Organic oxygen compound - Organic oxide - Primary alcohol - Hydrocarbon derivative - Organooxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as isoflavonoid o-glycosides. These are o-glycosylated derivatives of isoflavonoids, which are natural products derived from 3-phenylchromen-4-one.

External Descriptors

Not available

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